20112019

Research output per year

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Research Output

2019
2018

Implicit learning deficit in children with Duchenne muscular dystrophy: Evidence for a cerebellar cognitive impairment?

Vicari, S., Piccini, G., Mercuri, E., Battini, R., Chieffo, D., Bulgheroni, S., Pecini, C., Lucibello, S., Lenzi, S., Moriconi, F., Pane, M., D'Amico, A., Astrea, G., Baranello, G., Riva, D., Cioni, G. & Alfieri, P., Jan 16 2018, In : PLoS One. 13, 1, p. e0191164 10 p.

Research output: Contribution to journalArticle

2017

Cognitive profile in Duchenne muscular dystrophy boys without intellectual disability: The role of executive functions

Battini, R., Chieffo, D., Bulgheroni, S., Piccini, G., Pecini, C., Lucibello, S., Lenzi, S., Moriconi, F., Pane, M., Astrea, G., Baranello, G., Alfieri, P., Vicari, S., Riva, D., Cioni, G. & Mercuri, E., Dec 6 2017, In : Neuromuscular Disorders. 28, 2, p. 122-128 7 p.

Research output: Contribution to journalArticle

Psychopathological features in Noonan syndrome

Perrino, F., Licchelli, S., Serra, G., Piccini, G., Caciolo, C., Pasqualetti, P., Cirillo, F., Leoni, C., Digilio, M. C., Zampino, G., Tartaglia, M., Alfieri, P. & Vicari, S., Sep 28 2017, In : European Journal of Paediatric Neurology. 22, 1, p. 170-177 8 p.

Research output: Contribution to journalArticle

Visual perception skills: a comparison between patients with Noonan syndrome and 22q11.2 deletion syndrome

Piccini, G., Menghini, D., D'Andrea, A., Caciolo, C., Pontillo, M., Armando, M., Perrino, F., Mandolesi, L., Salerni, A., Buzzonetti, L., Digilio, M. C., Zampino, G., Tartaglia, M., Benassi, M., Vicari, S. & Alfieri, P., Jul 1 2017, In : Genes, Brain and Behavior. 16, 6, p. 627-634 8 p.

Research output: Contribution to journalArticle

2016

Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia

Barresi, S., Niceta, M., Alfieri, P., Brankovich, V., Piccini, G., Bruselles, A., Barone, M. R., Cusmai, R., Tartaglia, M., Bertini, E. & Zanni, G., 2016, (Accepted/In press) In : Clinical Genetics.

Research output: Contribution to journalArticle

2015

A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal Dysplasia

Zanni, G., Kalscheuer, V. M., Friedrich, A., Barresi, S., Alfieri, P., Di Capua, M., Haas, S. A., Piccini, G., Karl, T., Klauck, S. M., Bellacchio, E., Emma, F., Cappa, M., Bertini, E. & Breitenbach-Koller, L., Dec 1 2015, In : Human Mutation. 36, 12, p. 1155-1158 4 p.

Research output: Contribution to journalArticle

2014

Behavioral profile in RASopathies

Alfieri, P., Piccini, G., Caciolo, C., Perrino, F., Gambardella, M. L., Mallardi, M., Cesarini, L., Leoni, C., Leone, D., Fossati, C., Selicorni, A., Digilio, M. C., Tartaglia, M., Mercuri, E., Zampino, G. & Vicari, S., 2014, In : American Journal of Medical Genetics, Part A. 164, 4, p. 934-942 9 p.

Research output: Contribution to journalArticle

2012

Attention deficit hyperactivity disorder and cognitive function in duchenne muscular dystrophy: Phenotype-genotype correlation

Pane, M., Lombardo, M. E., Alfieri, P., D'Amico, A., Bianco, F., Vasco, G., Piccini, G., Mallardi, M., Romeo, D. M., Ricotti, V., Ferlini, A., Gualandi, F., Vicari, S., Bertini, E., Berardinelli, A. & Mercuri, E., Oct 2012, In : Journal of Pediatrics. 161, 4

Research output: Contribution to journalArticle

2011

Long term memory profile of disorders associated with dysregulation of the RAS-MAPK signaling cascade

Alfieri, P., Cesarini, L., Mallardi, M., Piccini, G., Caciolo, C., Leoni, C., Mirante, N., Pantaleoni, F., Digilio, M. C., Gambardella, M. L., Tartaglia, M., Vicari, S., Mercuri, E. & Zampino, G., May 2011, In : Behavior Genetics. 41, 3, p. 423-429 7 p.

Research output: Contribution to journalArticle